pharmacology Flashcards

1
Q

what are the benefits of using more than one drug during treatment

A
  • enhance therapeutic benefit
  • minimize drug toxicity
  • minimize drug-induced resistance
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2
Q

multi drug approach for HIV:

what are the drugs, and what are their targets

A
  • HIV binding, CCR5 antagonist = maraviroc
  • HIV fusion (bind to gp41) = enfuvirtide
  • NRTIs/NNRTIs = zidovudine/nevirapine
  • integrase inhibitors = raltegravir
  • protease inhibitors (maturation) = saquinavir
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3
Q

explain what pharmacokinetic boosting is and give example

A

enhancing the efficacy of a drug by adding another drug

- eg. giving ritonavir (potent inhibitor of Cyp3a4) with lopinavir

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4
Q

explain the combination therapy for HCV

A

sofosbuvir + PEG-interferon + ribavarin

Sofosbuvir + ribavirin

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5
Q

Action of sofosbuvir

A

nucleotide inhibitor of NS5B (RNA dep RNA polymerase)

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6
Q

empiric treatment of staph aureus or enterococcus faecalis and the drug action

A

gentamicin+penicillin
gentamycin - protein synthesis inhibition
penicillin - cell wall inhibition

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7
Q

explain the drug synergy of flucytosine and amphotericin

A

amphotericin b destroys the cell wall so flucytosine can more easily access the ribosome

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8
Q

explain the drug synergy in the treatment of pseudomonas jiroveci

A

sulfonamides and trimethoprim both act and two different parts of the folate pathway

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9
Q

explain the drug synergy in the treatment of testicular cancer

A

cisplatin and bleomycin = cause DNA damage/strand breaks

etoposide = inhibition of repair of the breaks

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10
Q

what are the 6 targets for for immunosuppression and what is a drug name for each

A
  • glucocorticoids = prednisolone
  • cytotoxic drugs = azathioprine
  • calcineurin inhibitor = cyclosporin
  • targeting cytokine receptors or cytokine = daclizumab
  • t-lymphocyte depletion = anti-thymocyte globulin
  • co-stimulation block = abatacept
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11
Q

explain the “induction” and “maintenance” immunosuppressant regimens

A

induction - T cell depletion (antibody mediated)

maintenance - calcineurin inhibitor, glucocorticosteroid, cytotoxic drug

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12
Q

how does genomic variation lead to a change in phenotype/drug responsitivity

A
  • change in protein structure and or function

- change in gene transcription and hence quantity of protein produced

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13
Q

how does SNPs affect statin metabolism

A

SNP in SLCO1B1 gene reduces statin uptake ==> enhancing toxitiy

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14
Q

what are the two major mutations leading to non-small cell lung cancer and what are the drugs that treat them

A

EGFR mutation - gefitinib

ALK rearragement - crizotinib

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15
Q

which SNP predicts poor response to anti-leukotriene therapies

A

mutation in the promotor of 5-lipoxygenase gene

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16
Q

what is the future of pharmacogenetics/omics

A

will enable more effective and safer use of medicines in a patient specific way